Evaluation on activity of cytochrome p450 enzymes in turbot via a probe drug cocktail

Cytochrome P450s (CYPs) are the main catalytic enzymes for metabolism by a variety of endogenous and exogenous substrates in mammals, fish, insects, etc. We evaluated the application of a multidrug cocktail on changes in CYP1, CYP2, and CYP3 activity in Turbot Scophthalmus maximus. The probe drugs w...

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Veröffentlicht in:Journal of aquatic animal health. - 1998. - 26(2014), 4 vom: 04. Dez., Seite 272-7
1. Verfasser: Chang, Zhi-Qiang (VerfasserIn)
Weitere Verfasser: Li, Jian, Zhai, Qian-Qian
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Journal of aquatic animal health
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Antitubercular Agents Folic Acid Antagonists Muscle Relaxants, Central Nucleic Acid Synthesis Inhibitors Phosphodiesterase Inhibitors Caffeine 3G6A5W338E Dapsone mehr... 8W5C518302 Cytochrome P-450 Enzyme System 9035-51-2 Chlorzoxazone H0DE420U8G Rifampin VJT6J7R4TR
Beschreibung
Zusammenfassung:Cytochrome P450s (CYPs) are the main catalytic enzymes for metabolism by a variety of endogenous and exogenous substrates in mammals, fish, insects, etc. We evaluated the application of a multidrug cocktail on changes in CYP1, CYP2, and CYP3 activity in Turbot Scophthalmus maximus. The probe drugs were a combination of caffeine (5 mg/kg body weight), dapsone (5 mg/kg), and chlorzoxazone (10 mg/kg). After a single intraperitoneal injection of the cocktail, the concentration of all three probe drugs in the plasma increased quickly to a peak and then decreased gradually over 24 h. Pharmacokinetic profiles of the three probe drugs were determined using a noncompartmental analysis, and the typical parameters were calculated. In the assay for CYP induction, pretreatment with rifampicin significantly reduced the typical pharmacokinetic metrics for caffeine and chlorzoxazone, but not dapsone, indicating that the activity of CYP1 and CYP2 in turbot were induced by rifampicin
Beschreibung:Date Completed 09.03.2015
Date Revised 30.09.2020
published: Print
Citation Status MEDLINE
ISSN:1548-8667
DOI:10.1080/08997659.2014.938868